MeSH Browser

MeSH Supplementary: Rozin Hertz Goodman syndrome
Unique ID: C535876
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535876
Entry Term(s): Camptodactyly, joint contractures, facial skeletal defects; Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye
Registry Number: 0
Heading Mapped to: *Abnormalities, Multiple; *Contracture; *Eye Abnormalities; *Hand Deformities, Congenital; *Craniofacial Abnormalities
Frequency: 0
Source: Clin Genet. 1984;26(4):342-55; Am J Med Genet. 1998;77(1):28-30
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Rozin Hertz Goodman syndrome MeSH Supplementary Concept Data 2024